J&J Family of Companies
Sr. Manager, Clinical Science, Cardiopulmonary
J&J Family of Companies, Spring House, Pennsylvania, United States, 19477
Sr. Manager, Clinical Science, Cardiopulmonary
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. We are searching for the best talent for a Sr. Manager, Clinical Science, Cardiopulmonary to join our team in Raritan or Titusville, NJ or Spring House or Horsham, PA. Purpose:
The Clinical Scientist (CS) is a responsible member of a clinical team dedicated to the development and execution of clinical strategies and the clinical and operational implementation of a complex compound program. The CS provides active scientific contribution to a cross-functional clinical team developing a molecular entity. The CS provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes responsibility for coordinating completion of clinical study reports and supports preparation of relevant documents for regulatory filings. This role involves extensive team matrix interactions with colleagues from a number of different disciplines. The CS may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area. You Will Be Responsible For:
Supports preparation of clinical development plans, trial protocols, and supports the operations group with trial set up and monitoring and assists with completion of clinical study reports Assists Physicians in evaluation of adverse events (pre and post-marketing) for relationship to treatment and supports the interpretation and reporting of results Assists Regulatory Affairs in determining requirements for any corrective actions or health authority reporting Interprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions Responsible for data review in conjunction with other clinical team members Assists Regulatory Affairs in the development of drug regulatory strategies Participate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc. Reviews medical literature and related new technologies May be asked to lead the execution of contracts May be asked to assess medical publications emerging from the team and its affiliates May be responsible, with appropriate colleagues, for review of Company advertising and promotion Qualifications/Requirements:
Education: A minimum of a Bachelor's degree is required. An advanced degree (e.g., MS, RN, RD, PhD or PharmD) is preferred. Skills/Experience: A minimum of at least 8 years of clinical research and development experience within the pharmaceutical industry is required. Experience in cardiovascular or metabolic product development and cross company alliances is preferred. Significant experience with managing/supervising clinical trials, medical and data monitoring clinical research programs is required. Previous Clinical Scientist Experience or equivalent. Strong interpersonal and communication skills are essential. The expected pay range for this position is $137,000 to $235,750. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). Employees are eligible for the following time off benefits: Vacation - up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year Holiday pay, including Floating Holidays - up to 13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefits The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. This job posting is anticipated to close on August 12, 2025. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. We are searching for the best talent for a Sr. Manager, Clinical Science, Cardiopulmonary to join our team in Raritan or Titusville, NJ or Spring House or Horsham, PA. Purpose:
The Clinical Scientist (CS) is a responsible member of a clinical team dedicated to the development and execution of clinical strategies and the clinical and operational implementation of a complex compound program. The CS provides active scientific contribution to a cross-functional clinical team developing a molecular entity. The CS provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes responsibility for coordinating completion of clinical study reports and supports preparation of relevant documents for regulatory filings. This role involves extensive team matrix interactions with colleagues from a number of different disciplines. The CS may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area. You Will Be Responsible For:
Supports preparation of clinical development plans, trial protocols, and supports the operations group with trial set up and monitoring and assists with completion of clinical study reports Assists Physicians in evaluation of adverse events (pre and post-marketing) for relationship to treatment and supports the interpretation and reporting of results Assists Regulatory Affairs in determining requirements for any corrective actions or health authority reporting Interprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions Responsible for data review in conjunction with other clinical team members Assists Regulatory Affairs in the development of drug regulatory strategies Participate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc. Reviews medical literature and related new technologies May be asked to lead the execution of contracts May be asked to assess medical publications emerging from the team and its affiliates May be responsible, with appropriate colleagues, for review of Company advertising and promotion Qualifications/Requirements:
Education: A minimum of a Bachelor's degree is required. An advanced degree (e.g., MS, RN, RD, PhD or PharmD) is preferred. Skills/Experience: A minimum of at least 8 years of clinical research and development experience within the pharmaceutical industry is required. Experience in cardiovascular or metabolic product development and cross company alliances is preferred. Significant experience with managing/supervising clinical trials, medical and data monitoring clinical research programs is required. Previous Clinical Scientist Experience or equivalent. Strong interpersonal and communication skills are essential. The expected pay range for this position is $137,000 to $235,750. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). Employees are eligible for the following time off benefits: Vacation - up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year Holiday pay, including Floating Holidays - up to 13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefits The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. This job posting is anticipated to close on August 12, 2025. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.